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The Quality of Rare Disease Registries: Evaluation and Characterization.

Academic Article
Publication Date:
2016
abstract:
BACKGROUND: The focus on the quality of the procedures for data collection, storing, and analysis in the definition and implementation of a rare disease registry (RDR) is the basis for developing a valid and long-term sustainable tool. The aim of this study was to provide useful information for characterizing a quality profile for RDRs using an analytical approach applied to RDRs participating in the European Platform for Rare Disease Registries 2011-2014 (EPIRARE) survey. METHODS: An indicator of quality was defined by choosing a small set of quality-related variables derived from the survey. The random forest method was used to identify the variables best defining a quality profile for RDRs. Fisher's exact test was employed to assess the association with the indicator of quality, and the Cochran-Armitage test was used to check the presence of a linear trend along different levels of quality. RESULTS: The set of variables found to characterize high-quality RDRs focused on ethical and legal issues, governance, communication of activities and results, established procedures to regulate access to data and security, and established plans to ensure long-term sustainability. CONCLUSIONS: The quality of RDRs is usually associated with a good oversight and governance mechanism and with durable funding. The results suggest that RDRs would benefit from support in management, information technology, epidemiology, and statistics.
Iris type:
01.01 Articolo in rivista
Keywords:
rare disease; quality; survey
List of contributors:
Coi, Alessio; Santoro, Michele; Bianchi, Fabrizio
Authors of the University:
COI ALESSIO
SANTORO MICHELE
Handle:
https://iris.cnr.it/handle/20.500.14243/313566
Published in:
PUBLIC HEALTH GENOMICS (ONLINE)
Journal
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URL

http://www.karger.com/DOI/10.1159/000444476
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